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1.

Lung Ultrasound-Implemented Diagnosis of Acute Decompensated Heart Failure in the ED: A SIMEU Multicenter Study.

Pivetta E, Goffi A, Lupia E, Tizzani M, Porrino G, Ferreri E, Volpicelli G, Balzaretti P, Banderali A, Iacobucci A, Locatelli S, Casoli G, Stone MB, Maule MM, Baldi I, Merletti F, Cibinel GA; SIMEU Group for Lung Ultrasound in the Emergency Department in Piedmont..

Chest. 2015 Jul;148(1):202-10. doi: 10.1378/chest.14-2608.

PMID:
25654562
2.

Genomic quantitative real-time PCR proves residual disease positivity in more than 30% samples with negative mRNA-based qRT-PCR in Chronic Myeloid Leukemia.

Pagani IS, Spinelli O, Mattarucchi E, Pirrone C, Pigni D, Amelotti E, Lilliu S, Boroni C, Intermesoli T, Giussani U, Caimi L, Bolda F, Baffelli R, Candi E, Pasquali F, Lo Curto F, Lanfranchi A, Porta F, Rambaldi A, Porta G.

Oncoscience. 2014 Jul 23;1(7):510-21.

3.

Chromosome anomalies in bone marrow as primary cause of aplastic or hypoplastic conditions and peripheral cytopenia: disorders due to secondary impairment of RUNX1 and MPL genes.

Marletta C, Valli R, Pressato B, Mare L, Montalbano G, Menna G, Loffredo G, Bernardo ME, Vinti L, Ferrari S, Di Cesare-Merlone A, Zecca M, Lo Curto F, Locatelli F, Pasquali F, Maserati E.

Mol Cytogenet. 2012 Oct 1;5(1):39. doi: 10.1186/1755-8166-5-39.

4.

Deletion of chromosome 20 in bone marrow of patients with Shwachman-Diamond syndrome, loss of the EIF6 gene and benign prognosis.

Pressato B, Valli R, Marletta C, Mare L, Montalbano G, Lo Curto F, Pasquali F, Maserati E.

Br J Haematol. 2012 May;157(4):503-5. doi: 10.1111/j.1365-2141.2012.09033.x. No abstract available.

PMID:
22295858
5.

Comparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cells.

Valli R, Marletta C, Pressato B, Montalbano G, Lo Curto F, Pasquali F, Maserati E.

Mol Cytogenet. 2011 May 9;4:13. doi: 10.1186/1755-8166-4-13.

6.

Evaluating chromosomal mosaicism by array comparative genomic hybridization in hematological malignancies: the proposal of a formula.

Valli R, Maserati E, Marletta C, Pressato B, Lo Curto F, Pasquali F.

Cancer Genet. 2011 Apr;204(4):216-8. doi: 10.1016/j.cancergen.2011.02.002.

PMID:
21536241
7.

The mammary gland and the homeobox gene Otx1.

Pagani IS, Terrinoni A, Marenghi L, Zucchi I, Chiaravalli AM, Serra V, Rovera F, Sirchia S, Dionigi G, Miozzo M, Frattini A, Ferrari A, Capella C, Pasquali F, Lo Curto F, Albertini A, Melino G, Porta G.

Breast J. 2010 Sep-Oct;16 Suppl 1:S53-6. doi: 10.1111/j.1524-4741.2010.01006.x. Erratum in: Breast J. 2011 Sep-Oct;17(5):568. Mozzo, Monica [corrected to Miozzo, Monica]; Curto, Francesco L [corrected to Lo Curto, Francesco].

PMID:
21050313
8.

Molecular monitoring of residual disease in chronic myeloid leukemia by genomic DNA compared with conventional mRNA analysis.

Mattarucchi E, Spinelli O, Rambaldi A, Pasquali F, Lo Curto F, Campiotti L, Porta G.

J Mol Diagn. 2009 Sep;11(5):482-7. doi: 10.2353/jmoldx.2009.080150.

9.

The route to development of myelodysplastic syndrome/acute myeloid leukaemia in Shwachman-Diamond syndrome: the role of ageing, karyotype instability, and acquired chromosome anomalies.

Maserati E, Pressato B, Valli R, Minelli A, Sainati L, Patitucci F, Marletta C, Mastronuzzi A, Poli F, Lo Curto F, Locatelli F, Danesino C, Pasquali F.

Br J Haematol. 2009 Apr;145(2):190-7. doi: 10.1111/j.1365-2141.2009.07611.x.

PMID:
19222471
10.

The isochromosome i(7)(q10) carrying c.258+2t>c mutation of the SBDS gene does not promote development of myeloid malignancies in patients with Shwachman syndrome.

Minelli A, Maserati E, Nicolis E, Zecca M, Sainati L, Longoni D, Lo Curto F, Menna G, Poli F, De Paoli E, Cipolli M, Locatelli F, Pasquali F, Danesino C.

Leukemia. 2009 Apr;23(4):708-11. doi: 10.1038/leu.2008.369.

PMID:
19148133
11.

Clonal chromosome anomalies and propensity to myeloid malignancies in congenital amegakaryocytic thrombocytopenia (OMIM 604498).

Maserati E, Panarello C, Morerio C, Valli R, Pressato B, Patitucci F, Tassano E, Di Cesare-Merlone A, Cugno C, Balduini CL, Lo Curto F, Dufour C, Locatelli F, Pasquali F.

Haematologica. 2008 Aug;93(8):1271-3. doi: 10.3324/haematol.12748. No abstract available.

12.

Microhomologies and interspersed repeat elements at genomic breakpoints in chronic myeloid leukemia.

Mattarucchi E, Guerini V, Rambaldi A, Campiotti L, Venco A, Pasquali F, Lo Curto F, Porta G.

Genes Chromosomes Cancer. 2008 Jul;47(7):625-32. doi: 10.1002/gcc.20568.

PMID:
18398823
13.

Constitutional trisomy 8 mosaicism in primary myelofibrosis: relevance to clinical practice and warning for trisomy 8 studies.

Maserati E, Pressato B, Valli R, Patitucci F, Lo Curto F, Pasquali F, Minelli A, Danesino C, Marchetti M, Barosi G.

Cancer Genet Cytogenet. 2007 Nov;179(1):79-81. No abstract available.

PMID:
17981220
14.

Monosomy 7 in myeloid malignancies: parental origin and monitoring by real-time quantitative PCR.

Porta G, Maserati E, Mattarucchi E, Minelli A, Pressato B, Valli R, Zecca M, Bernardo ME, Lo Curto F, Locatelli F, Danesino C, Pasquali F.

Leukemia. 2007 Aug;21(8):1833-5. No abstract available.

PMID:
17460707
15.

Monitoring the isochromosome i(7)(q10) in the bone marrow of patients with Shwachman syndrome by real-time quantitative PCR.

Porta G, Mattarucchi E, Maserati E, Pressato B, Valli R, Morerio C, Zecca M, Panarello C, Locatelli F, Lo Curto F, Pasquali F.

J Pediatr Hematol Oncol. 2007 Mar;29(3):163-5.

PMID:
17356395
16.

Establishment and study of different real-time polymerase chain reaction assays for the quantification of cells with deletions of chromosome 7.

Mattarucchi E, Marsoni M, Passi A, Lo Curto F, Pasquali F, Porta G.

J Mol Diagn. 2006 May;8(2):218-24.

17.

Different real time PCR approaches for the fine quantification of SNP's alleles in DNA pools: assays development, characterization and pre-validation.

Mattarucchi E, Marsoni M, Binelli G, Passi A, Lo Curto F, Pasquali F, Porta G.

J Biochem Mol Biol. 2005 Sep 30;38(5):555-62.

PMID:
16202235
18.

Familial platelet disorder with propensity to acute myelogenous leukemia: genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies.

Minelli A, Maserati E, Rossi G, Bernardo ME, De Stefano P, Cecchini MP, Valli R, Albano V, Pierani P, Leszl A, Sainati L, Lo Curto F, Danesino C, Locatelli F, Pasquali F.

Genes Chromosomes Cancer. 2004 Jul;40(3):165-71.

PMID:
15138996
19.

Familial myelodysplastic syndromes, monosomy 7/trisomy 8, and mutator effects.

Maserati E, Minelli A, Menna G, Cecchini MP, Bernardo ME, Rossi G, De Filippi P, Lo Curto F, Danesino C, Locatelli F, Pasquali F.

Cancer Genet Cytogenet. 2004 Jan 15;148(2):155-8.

PMID:
14734230
20.

Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases.

Maserati E, Aprili F, Vinante F, Locatelli F, Amendola G, Zatterale A, Milone G, Minelli A, Bernardi F, Lo Curto F, Pasquali F.

Genes Chromosomes Cancer. 2002 Jan;33(1):93-7. Review.

PMID:
11746991
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